Healthcare QA Specialist

Ups Job; México; Presencial; MXN 500.000 - 700.000; Jornada completa

Descripción de la vacante

UPS Healthcare Precision Logistics in Mexico is seeking a QA Professional to monitor the Quality System at the distribution center and ensure compliance with drug and medical device regulations. You will train staff, draft SOPs, and support audits.

The role involves maintaining QA records, coordinating CAPA, and driving continuous improvement of quality systems. Preferred candidates hold a Science degree and QPIC/AQPIC designation, with strong GMP knowledge and regulatory experience in

Formación

• Experience with GMP and regulatory requirements in pharma/healthcare
• Strong documentation and recordkeeping skills
• Knowledge of quality management systems and NCR/change control processes

Responsabilidades

• Monitor overall Quality System status of the distribution center.
• Ensure compliance with drug, medical device, and local regulations.
• Train staff in GMP and SOPs.
• Write and revise Standard Operating Procedures as required.
• Coordinate corrective actions and preventive measures.
• Support regulatory audits and client audits; liaise with regulators.
• Maintain QA records, NCR reports, and change controls; follow up on actions.
• Investigate discrepancies and advise on corrective actions.
• Contribute to continuous improvement of Quality Systems.

Conocimientos

GMP

SOPs

Auditing

Educación

Bachelor's degree in Science

QPIC/AQPIC designation

Descripción del empleo

**Together, we are Marken, UPS Healthcare Precision Logistics.**As the clinical and advanced therapy part of UPS Healthcare, we reach patients faster, with greater scalability and access to new pathways throughout the supply chain. With our One UPS advantage and comprehensive service portfolio, including Polar Speed's in-network pharmacies, we are optimally positioned to keep our clients competitive in an increasingly complex market.**Job Summary**This position monitors the overall Quality System status of the distribution center. This position acts in compliance to drug, medical device, and local regulations. Ensures quality processes are maintained through the implementation of procedures, training, and regular inspections.**Responsibilities*** Ensures all staff is trained in their respective job functions, including GMP.* Writes and revises Standard Operating Procedures as required.* Conducts regular inspections of the facility and recordkeeping, including summarization and reporting of findings. Coordinate or assist with corrective actions and preventative measures.* Communicates with clients and provides information during external audits* Liaises with Health Canada officials during regulatory audits.* Provides feedback and assistance to Customer/Client QA related questions and concerns.* Monitors the processes and systems within the Department to ensure regulatory compliance and effective operation.* Investigates discrepancies and problems, and advise the appropriate individuals of the findings.* Assists in development of pro-active strategies as a preemptive measure against potential future problems with systems or processes.* Completes NCR reports and change control requests and provide necessary follow-up.* Performs maintenance, support, and continuous improvements of Quality Systems.* QPIC designation duties.**Qualifications*** Pharmaceutical, healthcare or food industry experience - Preferred* Quality Assurance experience - Preferred* Bachelor’s Degree in Science related field (or internationally comparable degree) required - Preferred* QPIC/AQPIC designation - Preferred**Art der Anstellung:**Unbefristet